Z-0696-2016 Class II Terminated
FDA device recall Z-0696-2016 was initiated by Global Healthcare Inc on January 6, 2016 and is designated Class II. Reason for recall: Firm was notified of a potential product defect related to kinking (flattening) of anesthesia extension tubes which may represent a potential health hazard. The recall status is terminated (terminated March 25, 2016). Affected quantity: 2,000 cases (100 individual units per case).
Recall Details
- Product Type
- Devices
- Report Date
- February 10, 2016
- Initiation Date
- January 6, 2016
- Termination Date
- March 25, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,000 cases (100 individual units per case)
Product Description
ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China
Reason for Recall
Firm was notified of a potential product defect related to kinking (flattening) of anesthesia extension tubes which may represent a potential health hazard.
Distribution Pattern
US Distribution to state of: GA only.
Code Information
Lot Number 1505201